z-logo
Premium
The paclitaxel‐eluting Coroflex™ please stent pilot study (PECOPS I): Acute and 6‐month clinical and angiographic follow‐up
Author(s) -
Unverdorben Martin,
Degenhardt Ralf,
Vallbracht Christian,
Wiemer Marcus,
Horstkotte Dieter,
Schneider Henrik,
Nienaber Christoph,
Bocksch Wolfgang,
Gross Michael,
Boxberger Michael
Publication year - 2006
Publication title -
catheterization and cardiovascular interventions
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.988
H-Index - 116
eISSN - 1522-726X
pISSN - 1522-1946
DOI - 10.1002/ccd.20731
Subject(s) - medicine , restenosis , stent , lesion , stenosis , target lesion , myocardial infarction , radiology , mace , angioplasty , surgery , cardiology , percutaneous coronary intervention
Background and Objectives : Various active stent coatings significantly reduce restenosis rates and target lesion revascularization compared to bare metal stents. Therefore, the procedural and 6‐month performance of the new paclitaxel‐eluting Coroflex™. Please stent was investigated. Methods : Ninety‐seven patients (66 ± 7.6 years, 34/97(35.1%) diabetics, 11/97(11.3%) unstable angina) were enrolled per protocol for elective single stent deployment into native coronary de‐novo or post‐PTCA restenotic lesions (stenosis: ≥ 70%, < 100%; reference diameter ≥ 2.25 mm and <3.3 mm; lesion length ≤ 16 mm) with 13/97(13.4%) lesion type A, 64/97(66%) type B1, 20/97(20.6%) type B2). The mean reference diameter was 2.88 ± 0.42 mm, the lesion length 10.03 ± 2.93 mm, and the minimal lumen diameter 0.64 ± 0.22 mm. Results : The success rates of procedure and study stent deployment were 100% and 94.8%, respectively. In 5/97(5.2%) two stents were implanted. Follow‐up was performed clinically in 86/87(98.9%) and angiographically in 77/87(88.5%) patients after 6.1 ± 0.7 months. Major adverse cardiac events occurred in 7/87(8%) 1/87(1.2%) subacute thrombosis 10.3hrs post procedure, 1/87(1.2%) myocardial infarction, 5/87(5.7%) target lesion revascularizations. The in‐segment stenosis declined from 78 ± 7.2% to 9.4 ± 6.2% after stenting increasing to 31.9 ± 18.6% at follow‐up. The in‐segment late loss and the late loss index were 0.47 ± 0.6 mm and 0.23 ± 0.29 resulting in 6/77(7.8%) in‐segment restenoses three each of which were located either within or beyond the stent structure. The outcome was neither influenced by the prevalence of diabetes ( p = 0.4), hypercholesterolemia ( p = 1), hypertension ( p = 1), overweight ( p = 1), nor by the family history of coronary artery disease ( p = 0.7). Conclusion : The data of the paclitaxel‐eluting Coroflex™. Please stent tested in PECOPS I are within the range other available paclitaxel‐eluting stent. © 2006 Wiley‐Liss, Inc.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom